Catheter balloon systems and methods

ABSTRACT

Apparatus and method are provided for treatment of a bifurcation of a body lumen. The apparatus includes an elongated catheter body having a proximal end and a distal end. A balloon is associated with the distal end of the balloon catheter. The balloon includes a main vessel balloon for treating a main vessel of the bifurcation, and a branch vessel balloon for treating a branch vessel of the bifurcation. The branch vessel balloon includes an accordion configuration capable of being expanded from an unexpanded collapsed accordion configuration to an expanded accordion configuration extending into the branch vessel.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a continuation of application Ser. No. 10/985,005,filed Nov. 10, 2004, which claims the benefit of priority of U.S.Provisional Application No. 60/518,870, filed-Nov. 12, 2003, entitled“STENT DELIVERY SYSTEMS”; U.S. Provisional Application No. 60/547,778,filed-Feb. 27, 2004, entitled “SIDE BALLOON STENT DELIVERY SYSTEMS”; andU.S. Provisional Application No. 60/548,868, filed-Mar. 2, 2004,entitled “STENT DELIVERY SYSTEMS,” the disclosures of which are herebyincorporated herein by reference.

This application is related to co-pending U.S. patent application Ser.No. 10/705,247, filed Nov. 12, 2003, co-pending U.S. patent applicationSer. No. 10/802,036, filed Mar. 17, 2004, co-pending U.S. patentapplication Ser. No. 10/834,066, filed Apr. 29, 2004; and co-pendingU.S. patent application Ser. No. 10/893,278, filed Jul. 19, 2004. Thecomplete disclosures of the above-referenced applications areincorporated herein by reference.

FIELD OF THE INVENTION

The present invention relates to the field of medical balloon cathetersand, more particularly, to systems for delivering a stent at or near abifurcation of a body lumen.

BACKGROUND OF THE INVENTION

Balloon catheters, with or without stents, are used to treat strictures,stenoses, or narrowings in various parts of the human body. Devices ofnumerous designs have been utilized for angioplasty, stents and graftsor combination stent/grafts. Varied catheter designs have been developedfor the dilatation of stenoses and to deliver prostheses to treatmentsites within the body lumen.

Illustrative procedures involving balloon catheters include percutaneoustransluminal angioplasty (PTA) and percutaneous transluminal coronaryangioplasty (PTCA), which may be used to reduce arterial build-up suchas caused by the accumulation of atherosclerotic plaque. Theseprocedures involve passing a balloon catheter over a guidewire to astenosis with the aid of a guide catheter. The guidewire extends from aremote incision to the site of the stenosis, and typically across thelesion.

The balloon catheter is passed over the guidewire, and ultimatelypositioned across the lesion.

Once the balloon catheter is positioned appropriately across the lesion,(e.g., under fluoroscopic guidance), the balloon is inflated, whichbreaks the plaque of the stenosis and causes the arterial cross sectionto increase. Then the balloon is deflated and withdrawn over theguidewire into the guide catheter, and from the body of the patient.

In many cases, a stent or other prosthesis must be implanted to providesupport for the artery. When such a device is to be implanted, a ballooncatheter which carries a stent on its balloon is deployed at the site ofthe stenosis. The balloon and accompanying prosthesis are positioned atthe location of the stenosis, and the balloon is inflated tocircumferentially expand and thereby implant the prosthesis. Thereafter,the balloon is deflated and the catheter and the guidewire are withdrawnfrom the patient.

Administering PTCA and/or implanting a stent at a bifurcation in a bodylumen poses further challenges for the effective treatment of stenosesin the lumen. For example, dilating a main vessel at a bifurcation maycause narrowing of the adjacent branch vessel. In response to such achallenge, attempts to simultaneously dilate both branches of thebifurcated vessel have been pursued. These attempts include deployingmore than one balloon, more than one prosthesis, a bifurcatedprosthesis, or some combination of the foregoing. However,simultaneously deploying multiple and/or bifurcated balloons with orwithout endoluminal prostheses, hereinafter individually andcollectively referred to as a bifurcated assembly, requires accurateplacement of the assembly. Deploying multiple stents requirespositioning a main body within the main vessel adjacent the bifurcation,and then attempting to position another stent separately into the branchvessel of the body lumen. Alternatives to that include deploying adedicated bifurcated stent including a tubular body or trunk and twotubular legs extending from the trunk. Some examples include U.S. Pat.No. 5,723,004 to Dereume et al., U.S. Pat. No. 4,994,071 to MacGregor,and U.S. Pat. No. 5,755,734 to Richter et al.

Additional bifurcation stent delivery systems that provide improvedreliable treatment at bifurcations are disclosed, for example, in U.S.Pat. No. 6,325,826 to Vardi et al. and U.S. Pat. No. 6,210,429 to Vardiet al. The contents of the '826 and '429 patents aforementioned patentsare incorporated herein by reference.

A need still exists for further improved devices and techniques fortreating a bifurcated body lumen. For example, a need further exists foradditional stent delivery systems that can be used with stents having abranch access side hole and/or an extendible branch portion.

The present invention is directed to devices and techniques for treatinga bifurcated body lumen including systems for delivering an endoluminalprosthesis at or near a bifurcation of a body lumen. Systems, devicesand techniques are disclosed comprising balloon catheters configured tosuccessfully and reliably deploy stents at a bifurcation in a bodylumen. Additionally, the balloon catheters can be employed as balloonangioplasty catheters to treat occlusions in blood vessels such as forinstance in percutaneous transluminal coronary angioplasty (PTCA)procedures.

According to one aspect, the present invention provides a catheterassembly for use in bifurcated vessels. The assembly includes anelongated catheter body having a proximal end and a distal end and aballoon associated with the distal end of the balloon catheter. Theballoon includes a main vessel balloon for treating a main vessel of thebifurcation, and a branch vessel balloon for treating a branch vessel ofthe bifurcation. The branch vessel balloon includes an accordionconfiguration capable of being expanded from an unexpanded collapsedaccordion configuration to an expanded accordion configuration extendinginto the branch vessel.

According to another aspect, the branch vessel balloon includesaccordion folds and the folds are substantially collapsed against eachother in the unexpanded configuration, and separated from each other inthe expanded configuration.

In another aspect, the catheter assembly includes a bifurcated stent,which is disposed on the balloon. In particular, the present inventionprovides a catheter assembly including a bifurcated stent, which has amain vessel portion and an extendible branch vessel portion. The branchvessel balloon is disposed substantially adjacent the extendible branchportion. Upon expansion, the branch vessel balloon expands theextendible branch vessel portion of the stent into the branch vessel.

In another aspect of the invention, the catheter includes an inflationlumen, and the balloon has an interior in fluid communication with theinflation lumen. More particularly, the inflation lumen comprises twoinflation lumens. The first inflation lumen is in fluid communicationwith the interior of the branch vessel balloon. The second inflationlumen is in communication with an interior of the main vessel balloon.

In another aspect of the invention, the branch and main vessel balloonsdescribed above comprise a unitary balloon, and in other embodiments,the branch vessel balloon is separate from the main vessel balloon.

According to another aspect, the present invention provides a catheterassembly, which includes a side sheath associated with the elongatedcatheter body. At least a portion of the side sheath extends along thedistal end of the catheter body and adjacent the branch vessel balloon.In some aspects of the invention, the branch vessel balloon is disposedon the side sheath. In another aspect of the invention, the side sheathis disposable in the branch vessel. Additionally, the main vesselballoon is disposable in the main vessel during placement of thecatheter assembly in a bifurcated vessel. The accordion configurationcan be oriented to expand in a direction substantially perpendicular toa longitudinal axis of the main vessel balloon. In a further aspect ofthe invention, the branch vessel balloon is located on the side sheathand oriented to expand in a direction substantially parallel to alongitudinal axis of the side sheath.

In another aspect, the branch vessel balloon comprises a herniation onthe main vessel balloon, and in another aspect, the present inventionprovides a catheter assembly which includes a side sheath. One end ofthe branch vessel balloon is slidably affixed to the side sheath.

According to an additional aspect, the profile of the accordion folds ofthe catheter assembly of the present invention is substantially eitherround, elliptical, square, hexagonal or octagonal when viewed along thedirection of inflation. Additionally, in other aspects, the profile ofthe accordion folds is substantially triangular or round when viewedperpendicularly to the direction of inflation.

In a further aspect of the invention, the accordion configurationincludes a plurality of fluidly connected cells connected in series. Theseries defines an axis of primary inflation. In another embodiment, thesuccessive cells have a different size from the preceding cells in theseries. In a further aspect, the cells are adapted to merge into asubstantially tubular structure when fully expanded.

According to yet another aspect, the present invention provides acatheter assembly for use in bifurcated vessels. The assembly includesan elongated catheter body having a proximal end and a distal end and aballoon associated with the distal end of the balloon catheter. Theballoon includes a main vessel balloon for treating a main vessel of thebifurcation and a branch vessel balloon for treating a branch vessel ofthe bifurcation. The branch vessel balloon comprises a plurality offluidly connected cells connected in series, the series defining an axisof primary inflation. When the branch vessel balloon is expanded,expansion along the axis of primary inflation is greater than expansionin a radial direction, which is substantially perpendicular to the axisof primary inflation.

A further aspect of the present invention provides a catheter assemblyhaving successive cells, which differ in size from the preceding cellsin the series. In another aspect, the cells are adapted to merge into asubstantially tubular structure when fully expanded.

According to another aspect, the present invention provides a method oftreating a bifurcation of a body lumen. The bifurcation includes a mainvessel and a branch vessel. The method includes introducing a balloonand stent assembly into the main vessel, the balloon having at least oneaccordion inflation portion, wherein the accordion inflation portioncomprises a plurality of accordion folds; positioning the assembly atthe bifurcation; and inflating the balloon to expand the stent in themain vessel.

A further aspect of the invention provides a method of treating abifurcation of a body lumen in which the step of inflating includesexpanding a portion of the stent outwardly toward the branch vessel.Another aspect provides a method in which the accordion configurationexpands the portion of the stent outwardly toward the branch vessel. Thebody lumen described above can be a blood vessel.

BRIEF DESCRIPTION OF THE DRAWINGS

The invention is herein described, by way of example only, withreference to the accompanying drawings. With specific reference now tothe drawings in detail, it is stressed that the particulars shown are byway of example and for purposes of illustrative discussion of thepreferred embodiments of the present invention only, and are presentedto provide what is believed to be the most useful and readily understooddescription of the principles and conceptual aspects of the invention.

FIG. 1 is a side view of an illustrative embodiment of a stent deliverysystem constructed in accordance with the present invention.

FIG. 2 is an enlarged side view taken of the distal portion of thesystem of FIG. 1.

FIG. 3 is a view of the stent delivery system of FIG. 1 in a bloodvessel shown approaching a bifurcation in the vessel without a stentmounted thereon in accordance with a method of the present invention.

FIG. 4 is a view of the system of FIG. 3, including a stent mountedthereon.

FIG. 5 is a view of the stent delivery system of FIG. 1 in a bloodvessel located at a bifurcation in the vessel without a stent mountedthereon in accordance with a method of the present invention.

FIG. 6 is a cross-sectional side view of the stent delivery system ofFIG. 1 with a stent mounted thereon and shown in the expanded condition.

FIG. 7 is an enlarged side view of an accordion balloon of the stentdelivery system of FIG. 1.

FIG. 8 is a perspective view of a portion of a stent delivery systemconstructed according to an alternative embodiment of the presentinvention.

FIG. 9 is a side view of the stent delivery system of FIG. 8 with acut-away view of a stent mounted thereon in an unexpanded condition.

FIG. 10 is a side view of the stent delivery system of FIG. 9 with acut-away view of a stent mounted thereon in an expanded condition.

FIG. 11 is side view of a stent delivery system according to anotherembodiment of the invention.

FIG. 12 is a side view of the stent delivery system of FIG. 11 with apartial cut-away view of a stent mounted thereon in an expandedcondition.

FIG. 13 is a partial cut-away view of another embodiment of a stentdelivery system with a slidable accordion balloon partially expanded.

FIG. 14A is a partial cut-away view of the system shown in FIG. 13 withthe accordion balloon further partially expanded.

FIG. 14B is a partial cut-away view of the system shown in FIG. 14A withthe accordion balloon further expanded.

FIG. 15 is a side view of a stent delivery system according to anotherembodiment of the invention in an expanded condition.

FIG. 16 is side view of the stent delivery system of FIG. 15 with apartial cut-away view of a stent in an expanded condition.

FIG. 17 is a side view of the stent delivery system of FIG. 15 with apartial cut-away view of a stent in an unexpanded condition.

FIG. 18 is a cross-sectional view an embodiment of a delivery system inaccordance with the present invention.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

The present invention relates to balloon catheters such as balloonangioplasty catheters to treat occlusions in blood vessels. The ballooncatheters can be used alone or with a stent, prosthesis or graft. Such astent delivery system can be used for placement of a stent in a bodylumen, particularly at vessel bifurcations. A preferred stent to bedelivered is generally configured to at least partially cover a portionof a branch vessel as well as a main vessel. In general, a wide varietyof stents and deployment methods may be used with the stent deliverysystem embodiments of the present invention and the present inventionshould be understood to not be limited to any particular stent design orconfiguration. Examples of the types of stents that may be used with thedelivery systems of the present invention are disclosed, for example, inU.S. Pat. No. 6,210,429 to Vardi et al., U.S. Pat. No. 6,325,826 toVardi et al., and U.S. Patent Publication No. US2004-0138737, entitled“Stent With a Protruding Branch Portion For Bifurcated Vessels,” andU.S. Publication No. US2004-0212940, entitled “Stent With ProtrudingBranch Portion for Bifurcated Vessels,” the entire contents of which areincorporated herein by reference. In general, the aforementioned stentincludes a branch portion located at some point along the length of thestent that is configured to be extendible into a branch vessel in avessel bifurcation. Once the stent is in position in the main vessel andthe branch portion is aligned with the side branch vessel the stent canbe expanded and the delivery system in accordance with the principles ofthe invention is particularly adapted to expand the stent branch portioninto the side branch vessel. The stent, including the branch portion,may be expanded with a single expansion or multiple expansions.

The balloon catheter system and stent delivery system and methods of usein accordance with the principles of the invention are directed to atype that treats bifurcations in the vasculature, for example, where abranch vessel extends from a main vessel. The system provides for thebranch balloon to extend into the branch vessel and, preferably, deployan extendible branch portion of a stent into the branch vessel asdisclosed in the patents and applications discussed above, for example.Embodiments of the systems and methods are discussed more fully herein.In general, however, in accordance with the principles of the invention,balloon expansion into the branch vessel and, more particularly, toexpand the branch stent structure into the branch vessel, can beaccomplished by way of an accordion balloon as described and illustratedherein. The accordion balloon is constructed to be expandable,predominantly axially, e.g., along its axis of primary inflation,allowing it to extend into the branch vessel and/or deploy theextendible branch structure of the above-described stent.

In accordance with the principles of the invention, embodiments of theaccordion balloon are shown and described herein. In certainembodiments, the accordion balloon can be associated or integral withthe side sheath catheter. Alternatively the accordion balloon can beassociated or integral with the main balloon catheter as described inmore detail in the following. Additionally, in certain embodiments (see,e.g., FIGS. 11-17) the accordion balloon can be slidably attached to thecatheter or sheath to accommodate the axial or longitudinal expansion ofthe accordion balloon.

An illustrative view of one embodiment of a stent delivery system 10constructed in accordance with the present invention is shown in FIG. 1.Stent delivery system 10 generally comprises an elongate main cathetershaft 12 extending from a proximal end 14 to a distal end 16. As bestseen in FIG. 2, distal end 16 has a bifurcated tip structure with twobranch portions, a main vessel branch portion 18 and a side branchsheath 20 that branches off of main catheter shaft 12.

Balloon 26 generally includes an inflatable portion 32 comprising anaccordion balloon, as discussed in more detail in the following. Balloon26 as shown can be a bifurcated balloon, which is attached to mainvessel branch portion 18 adjacent the distal end 16 and comprises firstand second branch portions 27, 30. First branch portion 27 of balloon 26comprises an elongate inflatable portion 28. Second branch portion 30 ofballoon 26 comprises the second inflatable portion or auxiliaryinflatable portion 32 comprising the accordion balloon. Second branchportion 30 includes an inflation lumen that branches off from firstbranch portion 27 proximally from the balloon 26 and extendssubstantially adjacent elongate inflatable portion 28. The distal end ofsecond branch portion 30 is attached to first branch portion 27 at alocation distally from the balloon 26. In one preferred embodiment, thedistal end of branch portion 30 is fixedly attached distally of balloon26 in order to prevent at least the second inflatable portion 32 frommoving around the first branch portion 27, although in alternateembodiments it may be removably attached.

In a preferred embodiment, first inflatable portion 28 is generallycylindrical and extends coaxially along main vessel branch portion 18.Second inflatable portion 32 may have an accordion shape and sizeadapted to extend into the branch vessel as shown and described herein.For example, portion 32 may have a generally offset configuration andmay be positioned adjacent or in abutting relation with respect toelongate inflatable portion 28.

The first and second inflatable portions can have varied shapes, sizesand positioning in accordance with the principles of the invention. Forexample, in alternative design variations, accurate sizing andpositioning of the inflatable portions relative to the vessel may beachieved.

According to the present invention, the inflatable portions, orballoons, can be constructed of any suitable material. Preferably, theyare made of non-compliant materials. The balloons may be constructed ofan appropriate polymeric material. Particular examples include thepolyamide family, or the polyamide blend family, polyethylene (PE),polyethylene terephthalate (PET), polyurethanes, polyamides, andpolyamide blends such as PBAX. The compliance of the first inflatableportion 28 and the second inflatable portion 32 can be the same ordifferent. In one preferred embodiment, second inflatable portion 32 islongitudinally positioned at a generally central location relative tothe first inflatable portion 28. In alternate embodiments, secondinflatable portion 32 may be positioned at any position adjacent firstinflatable portion 28.

In a preferred embodiment, balloon branch portions 27 and 30 have acommon inflation lumen 34. Inflation lumen 34 can be conventional, andextend from a portion of the stent delivery system which always remainsoutside of the patient (not pictured). Inflation lumen 34 extendsdistally into each of first and second branch portions 27 and 30 andthus, inflation lumen 34 is in fluid communication with the interiors offirst inflatable portion 28 and second inflatable portion 32. Thusinflation lumen 34 is used to supply pressurized inflation fluid tofirst inflatable portion 28 and second inflatable portion 32 when it isdesired to inflate balloon 26. Inflation lumen 34 is also used to draininflation fluid from first inflatable portion 28 and second inflatableportion 32 when it is desired to deflate the balloon. First and secondinflatable portions are initially deflated when directing the stentdelivery device to the bifurcation lesion in a patient. In thisembodiment, the inflation lumen 34 inflates inflatable portions 28, 32substantially simultaneously. In an alternative embodiment, branchballoon portions 27 and 30 have separate inflation lumens. In thisalternative embodiment inflatable portions 28 and 32 can be inflatedsimultaneously or sequentially. When sequential inflation is desired,preferably, the first inflatable portion 28 is inflated first, followedby the inflation of the second portion 32.

First main guidewire lumen 22 extends through main vessel branch portion18 and first inflatable portion 28. Although first guidewire lumen 22extends through first inflatable portion 28 in the embodiment depictedin FIGS. 1-2, it is distinct from inflation lumen 34 and is not in fluidcommunication with the interior of balloon 26 as shown. Preferably, thefirst guidewire lumen 22 extends distally of first inflatable portion 28and has an open distal end. Alternatively, guidewire lumen 22 can extendthrough branch portion 30.

In the embodiment depicted in FIGS. 1-2, an optional side sheath 20 isillustrated which does not include an inflatable balloon. However, inalternate embodiments side sheath 20 could include an inflatable portionas discussed in more detail below and in co-pending U.S. patentapplication Ser. No. 10/644,550 entitled “Stent With A Protruding BranchPortion for Bifurcated Vessels,” for example. Side sheath 20 can beexterior to and distinct from inflation lumen 34 and, if so, would notbe in fluid communication with the interior of balloon 26 as shown. Asshown in the embodiment of FIGS. 1-2, side sheath 20 preferably extendsdistally of balloon 26, and may include a proximal open end 37 at anypoint along the length of the stent delivery system and a distal openend 39. Side sheath 20 can be of the type as described in U.S. Pat. No.6,325,826 to Vardi, et al., for example, and in operation the sidesheath 20 can extend through a branch access hole of the stent.

With reference to FIGS. 3-6, an exemplary manner of practicing theinvention will now be discussed. Referring to FIGS. 3 and 5, thedelivery system is shown in relation to an exemplary body lumen adjacenta blood vessel bifurcation 40 usually comprised of plaque and thedelivery system 10 is shown without a stent mounted thereon (FIGS. 3 and5). FIGS. 4 and 6 show the stent delivery system 10 with a stent 50mounted thereon.

Bifurcation 40 includes a main vessel 42 and a branch vessel 44.Illustrative obstructions 46 located within bifurcation 40 may span orat least partially obstruct main vessel 42 and a proximal portion branchvessel 44. Generally, stent delivery system 10 may be threaded over afirst main guidewire placed in the main vessel to guide the deliverysystem to the treatment site. More specifically, the proximal end offirst guidewire 36 is threaded into the distal open end of the mainguidewire lumen 22 and the delivery system is tracked to a position ator near bifurcation 40, as depicted in FIG. 3. Second guidewire 38 (FIG.5) is then threaded into stent delivery system 10 from the proximal endof the delivery system. More specifically, second guidewire 38 isthreaded into the open proximal end 37 of side sheath 20, and may extendtherefrom through the open distal end 39 of side sheath 20, as depictedin FIG. 5. Alternatively, second guidewire 38 can be resting dormant onthe inside of the side sheath, and when the system is proximal thebifurcation 40, it can be advanced out of side sheath 20 into sidebranch vessel 44. The systems in accordance with the principles of theinvention may be used in over-the-wire or rapid exchange systems, whichmay include rapid exchange on either or both of the side sheath or maincatheter. Rapid exchange is described in one exemplary embodiment inUS2003/0181923 to Vardi et al., published Sep. 25, 2003, the entirecontents of which are incorporated herein by reference.

In one embodiment, the stent delivery system 10 is positioned nearbifurcation 40, and with the distal end 16 (FIG. 1) positioned near sidebranch vessel 44 (FIGS. 3-6), second guidewire 38 is advanced into sidebranch vessel 44 from side sheath 20. Then, the first and secondinflatable portions of balloon 26 are positioned adjacent the opening ofside branch vessel 44 such that auxiliary inflatable side portion 32 ofbifurcated balloon 26 is aligned with side branch vessel. In oneexemplary embodiment, alignment may be achieved using markers, asdescribed in U.S. Pat. No. 6,692,483 to Vardi, et al., the entirecontents of which is incorporated herein by reference. Second guidewire38 remains in side branch sheath 20, and the distal end 16 of system 10remains in main vessel 42. First guidewire 36 remains within firstguidewire lumen 22, and may be further advanced and positioned in mainbranch vessel 42.

Once the system is properly positioned, pressurized fluid is supplied tofirst and second inflatable portions 28 and 32, respectively, of balloon26 to dilate the body lumen and expand a stent mounted thereon (FIG. 6).Preferably, the inflatable portion 28 expands the main body of the stentand inflatable portion 32 expands the side (opening) and expandablebranch structure of the stent, as discussed in more detail withreference to FIG. 6. After inflatable portions 28 and 32 have beeninflated as described above, balloon 26 is deflated by draining theinflation fluid via inflation lumen 34. This allows the inflatableportions 28 and 32 to collapse in preparation for withdrawal of theassembly from vessel 42.

Referring now to FIGS. 4 and 6, one preferred embodiment is shown withstent delivery system 10 and an exemplary stent 50 mounted on theexterior of distal end 16 of the stent delivery system. Stent 50includes an extendible branch portion 52 configured to extend into abranch vessel as discussed, for example, in U.S. Pat. No. 6,210,429 andin co-pending U.S. application Ser. No. 10/644,550, entitled “Stent withProtruding Branch Portion for Bifurcated Vessels”. The second inflatableportion 32 may be configured and positioned to deploy the outwardlyexpanding stent elements or branch portion 52 and may be positionedadjacent to the branch portion 52, or into a side branch access openingin the stent. As shown in FIG. 6, when first and second inflatableportions 28 and 32 are expanded, they simultaneously or sequentially,depending upon the configuration of the inflation lumen, cause the stent50 to expand in the main vessel 42 and the branch portion 52 of stent 50to be pushed or extended into the branch vessel 44. Upon inflation ofthe balloon 26, the second inflatable portion 32 expands and extends thebranch portion 52 toward the branch vessel to open and support theentrance or ostium of the side branch artery. This would occursimultaneously when the balloons share a common inflation lumen butcould be sequentially if separate inflation lumens are used. Although abifurcated balloon is depicted, as shown, more than two inflatableportions or more than two balloons may be utilized with the presentinvention, or a single balloon can be used herein as discussed withreference to FIGS. 12-14.

Further, although the second inflatable portion 32 of the embodimentillustrated in FIGS. 1-6 are shown as being centrally located on thesecond branch portion 30, it should be noted that the inflatable portion32 may be located at any desired position along the length of the secondbranch portion 30. For example, once associated with a stent, itpreferably can be placed such that it corresponds to the location alongthe middle ⅓ of the stent, or, adjacent the extendible branch structure.

As illustrated, for example, in FIGS. 5 and 6, the first and secondbranch portions 27 and 30 have a longitudinal axis A. The longitudinalaxes are substantially parallel with each other. The term “substantiallyparallel” is intended to encompass deviations from a purely parallelrelationship which may be caused by flexure of the branch portions 27and 30, or other components, experienced during insertion, travel, anddeployment within a body lumen.

Referring now to FIG. 7, the accordion feature will now be described inmore detail with reference to an exemplary embodiment. FIG. 7 is anenlarged view of inflatable side portion 32 of bifurcated balloon 26 asdepicted in FIGS. 1-6. The inflatable side portion 32 is constructed toextend laterally outwardly from a longitudinal axis of the system andinto the branch vessel. As shown, the inflatable side portion 32 has agenerally “accordion” shape in that it includes a series of fluidlyconnected cells 60. The accordion cells 60 preferably have a broadcentral portion 64 which tapers to narrower end portions 62. Thus, whenviewed in profile, the cells 60 typically have a “flattened” hexagonshape when inflated. However, the shape of the profile is not critical.For example, the profile of the cells 60 may have a more rounded shape.Further, the accordion structure 33 may be constructed so that uponmaximum inflation, the individual cells 60 merge, resulting in agenerally tubular structure. When deflated, the cells collapse into alow profile configuration as discussed in more detail in the following.

The individual cells 60 are fluidly connected via the narrow endportions 62. Thus, fluid entering the first cell 60 of the inflatableside portion 32 of the balloon 26 passes to successive cells 60 in theseries of cells 60 comprising the inflatable side portion 32, creatingan axis of primary inflation from the first cell 60 to the final cell60. In this manner, the inflatable side portion 32 can expand to agreater extent along the axis of primary inflation than in the radialdirection perpendicular to the axis of primary inflation. As such in theunexpanded condition, the balloon is substantially flat, e.g., a flatflexible disc shape, and in the expanded configuration the balloonlength significantly increases along the axis of primary inflation. Bycomparison, for example, the main balloon 28 has a relatively fixedlongitudinal length that remains substantially unchanged upon expansion.

When viewed along the axis of primary inflation, the cells 60 arepreferably round. However, any shape may be used. For example, the cells60 may be, but are not limited to being, elliptical, square, hexagonalor octagonal. Further, successive cells 60 need not be the same size.For example, successive cells 60 may decrease or increase in size fromthe preceding cell 60, resulting in a tapered inflatable side portion32.

The components of the auxiliary inflatable side portion 32 may be sizedappropriately, as will be readily apparent to those skilled in the art.The accordion structure 33 can be provided with a suitable inflated celldiameter and connector diameter. The diameters can vary according tovarious factors known to those skilled in the art. Further, theauxiliary inflatable side portion 32 can comprise any number of cells 35as determined for the particular application. Additionally, theexpansion of the second inflatable portion 32 produces a force and aconfiguration to deploy a branch portion 52 of a stent 50 into a sidebranch vessel 44. Accordingly, second inflatable portion 32 may unfoldor push out the branch portion 52 of the stent while controlling orlimiting the radial expansion as desired.

Branch vessel inflatable portion 32, as discussed above and as shown,includes an embodiment of the accordion feature and other embodimentsare shown herein and discussed in the following. The accordionconfiguration of the inflatable portion 32, however, can includedifferent shapes, sizes and construction in accordance with theprinciples of the invention. For example, the accordion feature can becombined with the embodiments disclosed in U.S. Provisional PatentApplication Ser. No. 60/518,870, entitled “Stent Delivery Systems.”Also, the accordion principles discussed above with reference to FIGS.1-7 apply to the other embodiments discussed herein.

FIG. 8 illustrates an alternative embodiment of the present inventionalso for use in the treatment of branch arteries, including alone or,for example, by incorporation into stent delivery systems of the typepreviously described. The balloon depicted in the embodiment of FIG. 8can be referred to as a “herniated” accordion balloon configuration thatfunctions in a manner similar to the embodiments described above. Theherniated accordion balloon configuration is characterized by having agenerally cylindrical shape in an unexpanded configuration, and agenerally cylindrical shape with a generally accordion shaped appendagethat inflates outwardly relative to the longitudinal axis of the balloontoward the branch artery in an expanded state or configuration. Thisprotrusion can be referred to as a herniation, bulge, protrusion, orextension, for example. The particular shape, size, and configuration ofthe balloon and the accordion herniations illustrated herein areexemplary, and may be modified from that explicitly shown and described.The expandable herniation, bulge, protrusion, or extension can beexpandable towards the entrance of side branch (see, e.g., 44, FIG. 3)over a suitable dimension, such as 1-4 mm.

The embodiment of the balloon depicted in FIG. 8 can be utilized in amanner similar to that which has been described in connection withpreviously illustrated embodiments (see, e.g., FIGS. 1-7). With regardto the embodiment depicted in FIG. 8, it should be understood that theherniated accordion balloon construction depicted herein can be usedalone or can be substituted for the entire bifurcated balloon (e.g. 26,FIGS. 1-7) or a portion of the bifurcated balloon (e.g., 32) withcertain modifications, as needed, in accordance with the principles ofthe invention.

An exemplary embodiment of a herniated accordion balloon catheter 526 isillustrated in FIG. 8. In the illustrated embodiment, the herniatedballoon catheter 526 comprises a balloon 527 having an elongatedinflatable portion 528 and an accordion herniation, bulge, protrusion,or extension 532. In the embodiment of FIG. 8 the balloon catheter 526further includes a lumen 534 which can serve to communicate pressure forinflation of the balloon 527, and provide a passageway for a guide wire,etc.

The particular configuration and dimensions of the balloon 527 can varyaccording to a number of factors. For purposes of illustration only,certain suitable, but non-limiting, dimensions of various components ofthe balloon 527 will now be described. The balloon 527 can be providedwith a length dimension L₁ which is about 4-100 mm. The balloon can beprovided with an outside diameter OD₁ which is on the order of about1-10 mm.

Although the accordion herniation 532, of the embodiment illustrated inFIG. 8 are shown as being centrally located on the herniated balloon527, it should be noted that the herniation 532 maybe located at anydesired position along the length of the balloon. For example, onceassociated with a stent, it can preferably be placed such that itcorresponds to the location along the middle ⅓ of the stent and/oradjacent the extendible branch structure of the stent.

The balloon 527 can be constructed of any suitable material such asthose previously disclosed herein. In addition, the balloon 527, as wellas any other embodiments described herein, can be constructed of acomposite material. Suitable materials include a combination ofelastomeric and semi to non-compliant materials such as: urethane;silicone; nylon; latex; (elastomeric) polyethylene hytrel pebaxpolyaryletherthketone; polyoxymethylene; polyamide; polyesterthermoplastic polyetheretherkatone; and polypropylene (seminon-compliant). The balloon 526, can be also be constructed by combiningthe above-disclosed materials with woven textile materials such asKevlar, silk, cotton, wool, etc. This can be accomplished by winding orweaving a textile material onto a rod that has the shape of the desiredaccordion herniated balloon. The polymer component of the composite isthen extruded or dip-coated over the rod. This composite structure isthen cured, heat set, or adhesively fused together. The rod is thenremoved and the remaining shape comprises the accordion herniatedballoon 527. Alternatively, this can be accomplished by combining theabove-described materials with woven material only on the main balloonportion and not on the accordion balloon portion, whereby uponapplication, by whatever process, the elastomeric or polyurethane, forexample, alone forms the accordion balloon portion.

The accordion herniation 532, can be provided by adding an appendage toa conventional balloon by using a molded collar or adhesively attachingan object to the surface of the balloon, or by using a mound of adhesiveto create the herniation.

The balloon 527 can be constructed by molding three small balloons andattaching them in tandem, the central balloon comprising the desiredshape of the accordion herniation. These balloons would share a commoninflation port. When the balloons are inflated, the center balloonexpands in the desired manner to form the accordion herniation.

FIG. 9 shows balloon 527 in a stent delivery system 600, of which onlythe distal end portion is shown. System 600 is shown in an unexpandedcondition. The distal end is shown at 602 and the proximal end at 604.The system 600 generally includes balloon 526, side sheath 620 andbifurcated stent 624, of the type discussed above. The stent is depictedgenerally and without detail for illustration. Side sheath 620 extendsthrough a side branch access opening in stent 624. In this figure, theunexpanded accordion herniation is shown at reference numeral 532. Whenunexpanded or collapsed, the accordion herniation 532 is a substantiallyflat configuration, for example, a flat flexible disc shape. Asillustrated, the unexpanded accordion herniation 532 is disposed againstthe side of balloon 526, such as by folding. However, it is notnecessary for the unexpanded accordion herniation 532 to be folded inthis manner. For example, the unexpanded accordion herniation 532 may befolded entirely on top of balloon 527. In fact, any folding techniquemay be used as long as the herniation 532 is capable of being expandedand, in particular, expanded to deploy branch portion 626. FIG. 10 showssystem 600 in an expanded condition with accordion herniation 532expanded to deploy branch portion 626 of stent 624 outwardly into abranch vessel (not shown).

As illustrated, the accordion herniation 532 in this embodiment and thesecond inflatable portion 32 in the previous embodiment are shown toexpand in a direction substantially perpendicular to the longitudinalaxis of the elongate inflatable potions 528, 28 of those respectiveembodiments. However, the accordion herniation 532 and the secondinflatable portion 32 may be fabricated to expand at any angle relativeto the elongate inflatable potions 528, 28 as required by the particularconfiguration of the vessels of the bifurcation to be treated.Additionally, in these embodiments the axis of inflation of theaccordion structure 33 is generally at an angle to the axis of theinflation lumen supplying air to the accordion structure 33.

Referring now to FIGS. 11-12, an alternative embodiment of a stentdelivery system 1190 is shown. Stent delivery system 1190 comprises anelongate main catheter shaft 1192 extending from a proximal end 1194 toa distal end 1196. Distal end 1196 can include a bifurcated structurewith two branch portions, a main vessel branch portion 1198 and a sidebranch sheath 1100. Main vessel branch portion 1198 itself can includetwo branches, a first branch 1104 which can include a balloon 1102 andan accordion branch portion 1106. Balloon 1102 can include an elongateinflatable portion 1108 that extends along first branch portion 1104 ofmain vessel branch portion 1198.

Accordion branch portion 1106 can extend between main vessel branchportion 1198 to about the distal end of side branch sheath 1100.Accordion branch portion 1106 can include a generally axially inflatableportion 1109, in particular, an accordion balloon. In general,inflatable portion 1109 is configured and designed such that uponinflation it expands or elongates along an axis, for example, itslongitudinal axis 1111.

In a preferred embodiment of the invention, the distal end of axiallyinflatable portion 1109 is slidably attached to side sheath 1100 whilethe proximal end can be secured to main vessel branch portion 1198.Portion 1109 can be slidably attached by any structure in accordancewith the principles of the invention, including, for example, a flexibletube.

In one method of slidable attachment, the distal end of axiallyinflatable portion 1109 may be fixedly attached to a tubular member 1110that is slidably received on the exterior of side sheath 1100. In apreferred embodiment, axially inflatable portion 1109 is generallyshaped and/or folded similar to an accordion and upon inflation,inflatable portion 1109 unfolds or expands in an axial direction, alongits longitudinal axis 1111. In this manner, the distal tip of inflatableportion 1109 slides in the distal direction along side sheath 1100.

In operation, when a stent 2136 is mounted on the delivery system 1190and delivered to a vessel bifurcation, outwardly deployable elements orbranch portions 2138 of the stent 2136 may be advantageously deployed byaxially inflatable portion 1109 (FIG. 12). Inflatable portion 1109 isdisposed within stent 2136 in the unexpanded configuration and isexpandable along its axis, e.g., its longitudinal axis, into the branchvessel. Because inflatable portion 1109 slides along side sheath 1100 inthe distal direction, an axial force is created in the direction of sidesheath 1100 that may more efficiently deploy a branch portion 2138 of astent 2136 into a side branch vessel. The axial force created may unfoldor push out the branch portion 2138 of the stent while controlling orlimiting the radial expansion as desired. As a result, a stent 2136 maybe designed having a branch portion that can more effectively treatlesions in a side branch vessel. For example, in some stent 2136 designsthe extendible branch portion 2138 of the stent 2136 may be extendedfurther into the branch using this delivery system configuration.

Referring to FIGS. 13, 14A and 14B, an alternative embodiment of anaccordion or axially inflatable balloon 2120 is shown. Balloon 2120extends coaxially along a catheter or sheath 2122. Sheath 2122 includesan inflation lumen 2130 for inflating balloon 2120 and a guidewire lumen2132 for receiving a guidewire. Inflation lumen 2130 is in fluidcommunication with balloon 2120 through balloon intake 2134. Proximalend 2124 of balloon 2120 is fixedly attached to sheath 2122 and distalend 2126 of balloon 2120 is fixedly attached to a tubular member 2128,which is slidably received on the exterior of sheath 2122. Tubularmember 2128 can be a flexible tube. Tubular member 2128 preferably has alength sufficient to be attached to the balloon material and sufficientto extend into the balloon 2120 to form a fluid-tight seal when balloon2120 is inflated. In particular, tubular member 2128 is constructed sothat, upon inflation, it is slidable along sheath 2122, yet the end ofsheath 2122 that is inside the balloon, when inflated, is pressedagainst sheath 2122 in an amount sufficient to create a fluid-tightseal. In operation, upon inflation, distal end 2126 is slidable alongsheath 2122, by way of tubular member 2128 to expand balloon 2120 from xamount of expansion as shown in FIG. 13, further to y amount ofexpansion as shown in FIG. 14A, even further to z amount of expansion asshown in FIG. 14B where x≦y≦z. In an alternative embodiment, not shown,both proximal and distal ends 2124, 2126 could be fixedly secured to asheath extending from the distal end and a sheath extending from theproximal end in accordance with the principles of the invention.

The embodiment of FIGS. 13, 14A and 14B can be used alone or incombination with other embodiments disclosed herein. For example, sheath2122 (FIGS. 13, 14A and 14B) may be part of a stent delivery system. Asshown in FIGS. 15-17, stent delivery system 2300 can include a sidesheath 2322, of the type described with reference to FIGS. 13, 14A and14B, and main balloon catheter 2302. Side sheath 2322 includes accordionballoon 2320 with tubular member 2328 as discussed above. FIG. 16 showsa stent 2324 mounted on system 2300 in an expanded condition, while FIG.17 shows a stent 2324 mounted on system 2300 in an unexpanded condition.When stent 2324 having a branch portion 2326 is mounted on the deliverysystem and delivered to a vessel bifurcation, sheath 2322 may extendthrough a side branch access hole of the stent 2324 with balloon 2320positioned adjacent an interior of the branch portion. As in theembodiment illustrated in FIGS. 13, 14A and 14B, the accordion balloon2320 may be folded in any manner that allows for deployment of thebranch portion 2326 of stent 2324. Upon inflation, balloon 2320 expandsaxially by tubular member 2328 sliding distally along sheath 2322 in thedistal direction creating an axial force along the axis of the sidesheath. The axial force created can expand or push out the branchportion 2326 of the stent 2324 into the branch vessel a sufficientdistance into the branch vessel and without unnecessarily expanding thebranch portion 2326 radially. As a result, a stent 2324 has a branchportion 2326 that can more effectively be used to treat lesions in aside branch vessel. For example, in some stent designs the extendiblebranch portion 2326 of the stent 2324 may be extended further into thebranch using this delivery system configuration.

In an alternative embodiment, the embodiments of FIGS. 11-17 canassociate the accordion balloon with side sheath so that upon expansionthe accordion balloon follows the side sheath into the side branchvessel.

Although the invention has been described for use with a singleaccordion balloon, the use of one or more accordion balloons iscontemplated as discussed, for example, in co-pending U.S. patentapplication Ser. No. 10/834,066, entitled “Catheter Balloon Systems andMethods.”

In an alternative embodiment, shown in FIG. 18, a first guidewire lumen3142 may not pass through the interior of first inflatable portion 3148.For example, the lumen may be affixed to the exterior of the balloon, orthe balloon may be formed with a plurality of folds through which theguidewire passes. Or the guidewire (not shown) may pass through thefolds of the balloon. In this embodiment, guidewire lumen 3142 isseparate from the inflation lumen 3154. In a preferred embodiment,guidewire lumen 3142 may have an abbreviated or shorter length ascompared to the inflation lumen 3154 thereby providing less lumen for aguidewire to pass through. The distal end of lumens 3142 and 3154 arepreferably attached together at the very distal tip of the deliverysystem, such as by bonding, and the proximal end of the guidewire lumenis connected to the inflation lumen. Thus, this stent deliveryembodiment is neither an “over the wire” system (the guidewire lumendoes not stay inside the inflation lumen through the entire length ofthe delivery system). Nonetheless, the abbreviated or shorter length ofguidewire lumen 3142 as compared to the inflation lumen 3154 allows, forexample, rapid insertion and removal of a guidewire therethrough. Thisfeature can be used on a delivery system regardless of the number of theballoons used, or whether the delivery system utilizes a side sheath.For example, this could be used alone or in combination with otherembodiments described herein.

While the invention has been described in conjunction with specificembodiments and examples thereof, it is evident that many alternatives,modifications and variations will be apparent to those skilled in theart upon reading the present disclosure. Accordingly, it is intended toembrace all such alternatives, modifications and variations that fallwithin the spirit and broad scope of the appended claims. Furthermore,features of each embodiment can be used in whole or in part in otherembodiments.

1. A stent delivery system comprising: a catheter having a proximal endand a distal end; a first balloon arrangement coupled to the catheteradjacent the distal end of the catheter, the first balloon arrangementincluding a main vessel balloon; a second balloon arrangement coupled tothe catheter adjacent the first balloon arrangement, the second balloonarrangement including a branch vessel balloon and an inflation lumen,the branch vessel balloon having an accordion configuration that isexpandable along a longitudinal axis from a collapsed configuration toan expanded configuration, the longitudinal axis extending radially awayfrom the inflation lumen.
 2. The stent delivery system as claimed inclaim 1, further comprising a stent arranged on the first balloonarrangement.
 3. The stent delivery system as claimed in claim 2, whereinthe stent has a main vessel portion and an extendible branch vesselportion, wherein the branch vessel balloon is disposed substantiallyadjacent the extendible branch portion, whereby upon expansion thebranch vessel balloon expands the extendible branch vessel portion ofthe stent into a branch vessel.
 4. The stent delivery system as claimedin claim 1, wherein the catheter includes an inflation lumen and thefirst balloon arrangement has an interior in fluid communication withthe inflation lumen.
 5. The stent delivery system as claimed in claim 1,wherein the first balloon arrangement is integrally formed with thesecond balloon arrangement.
 6. The catheter assembly of claim 1, whereinthe branch vessel balloon includes a plurality of fluidly connectedcells.
 7. The catheter assembly of claim 6, wherein the fluidlyconnected cells are connected in series.
 8. The catheter assembly ofclaim 7, wherein successive cells have a different size from thepreceding cell in the series.
 9. The catheter assembly of claim 6,wherein the cells are adapted to merge into a substantially tubularstructure when fully expanded.
 10. A stent delivery system comprising: acatheter having a proximal end and a distal end; a first balloon coupledto the catheter adjacent the distal end of the catheter; a firstinflation lumen configured to provide fluid to the first balloon; asecond inflation lumen arranged on the catheter adjacent the firstinflation lumen; a second balloon coupled to the catheter adjacent thefirst balloon, the second balloon having an accordion configuration thatis expandable along a longitudinal axis from a collapsed configurationto an expanded configuration, the longitudinal axis extending radiallyaway from the second inflation lumen; and a stent disposed on the firstballoon.
 11. The stent delivery system as claimed in claim 10, whereinthe stent has a main vessel portion and an extendible branch vesselportion, wherein the second balloon is disposed substantially adjacentthe extendible branch portion, whereby upon expansion the second balloonexpands the extendible branch vessel portion of the stent into a branchvessel.
 12. The stent delivery system as claimed in claim 10, whereinthe first balloon is integrally formed with the second balloon.
 13. Thecatheter assembly of claim 10, wherein the second balloon includes aplurality of fluidly connected cells.
 14. The catheter assembly of claim13, wherein the fluidly connected cells are connected in series.
 15. Thecatheter assembly of claim 14, wherein successive cells have a differentsize from the preceding cell in the series.
 16. The catheter assembly ofclaim 14, wherein the cells are adapted to merge into a substantiallytubular structure when fully expanded.